唐氏综合征成人体重指数变化与脂质过氧化

C.J. Chávez , P. Ortega , A. D’Escrivan , L.E. Miranda , J.Y. Leal M , C. Delgado
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引用次数: 2

摘要

引言和目的21三体或唐氏综合征(DS)是最常见的染色体遗传性智力低下的原因,其中肥胖是一个公共卫生问题。肥胖是一种与脂质过氧化和抗氧化机制改变有关的促氧化状态。基因剂量的影响与DS的氧化应激有关。本研究的目的是确定DS患者的脂质过氧化状态和体重指数(BMI)的变化。患者和方法对50名正常核型(NK)的成年受试者(31.0±6.3岁)和29名DS患者(28.0±8.7岁)进行了前瞻性和横断面研究,随机选择。用硫代巴比妥酸衍生物测定血清丙二醛(MDA)水平。在患有DS的成年人中测定BMI。使用SPSS 15统计程序对数据进行分析,使用95%CI,p<;。05.结果与成人NK组(0.5±0.4 nmol/ml)相比,患有DS的成人表现出高浓度的MDA(0.9±0.7 nmol/ml,p<;.009)。在患有DS的成人中,72.4%的BMI(n=21)出现异常。患有DS和超重(BMI=27.5±1.3)的成人中MDA浓度升高(1.3±1.0 nmol/ml),但患有DS的肥胖成人没有显著降低。结论尽管有报道称,在没有DS的严重肥胖成人中,抗氧化酶降低,基因剂量的作用可能是减少DS肥胖成人脂质过氧化的一个促进因素,而不是其病理后果的保护因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Body mass index changes and lipid peroxidation in adults with Down's syndrome

Introduction and objective

Trisomy 21 or Down's syndrome (DS) is the most common cause of mental retardation of chromosomal origin, in which obesity is a public health problem. Obesity is a pro-oxidant state associated with lipid peroxidation and alterations of antioxidant mechanisms. The effect of gene dosage has been linked to oxidative stress in DS. The objective of this study was to determine the status of lipid peroxidation and changes in body mass index (BMI) in adults with DS.

Patients and method

A prospective and cross-sectional study was conducted on 50 adult subjects (31.0 ± 6.3 years) with normal karyotype (NK) and 29 adults with DS (28.0 ± 8.7 years), randomly selected.The serum levels of malondialdehyde (MDA) were analysed by thiobarbituric acid derivatives. The BMI was determined in adults with DS. The data were analysed using the SPSS 15 statistical program, using a 95% CI, p<.05.

Results

Adults with DS showed high concentrations of MDA (0.9 ± 0.7 nmol / ml, p<.009) compared to adult NK group (0.5 ± 0.4 nmol / ml). Abnormality was observed in 72.4% of BMI (n = 21) of adults with DS. Elevated concentrations of MDA (1.3 ± 1.0 nmol / ml) were seen in adults with DS and overweight (BMI = 27.5 ± 1.3), showing no significant decrease in obese adults with DS.

Conclusion

Although a reduction of antioxidant enzymes in severely obese adults without DS has been reported, the effect of gene dosage may be a contributing factor in reducing lipid peroxidation in obese adults with DS, without being a protective factor of its pathological consequences.

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